학술논문
Effect of recombinant human bone morphogenetic protein-2 on bisphosphonate-treated osteoblasts
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- 영문명
- Effect of recombinant human bone morphogenetic protein-2 on bisphosphonate-treated osteoblasts
- 발행기관
- 대한구강악안면외과학회
- 저자명
- Taek-Kyun Kwon Jae-Min Song In-Ryoung Kim Bong-Soo Park Chul-Hoon Kim In-Kyo Cheong Sang-Hun Shin
- 간행물 정보
- 『대한구강악안면외과학회지』대한구강악안면외과학회지 제40권 제6호, 291~296쪽, 전체 6쪽
- 주제분류
- 의약학 > 내과학
- 파일형태
- 발행일자
- 2014.12.30

국문 초록
영문 초록
Objectives: Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is a side effect of bisphophonate therapy that has been reported in recent years.
Osteoclastic inactivity by bisphosphonate is the known cause of BRONJ. Bone morphogenetic protein-2 (BMP-2) plays an important role in the development of bone. Recombinant human BMP-2 (rhBMP-2) is potentially useful as an activation factor for bone repair. We hypothesized that rhBMP-2 would enhance the osteoclast-osteoblast interaction related to bone remodeling.
Materials and Methods: Human fetal osteoblast cells (hFOB 1.19) were treated with 100 μM alendronate, and 100 ng/mL rhBMP-2 was added.
Cells were incubated for a further 48 hours, and cell viability was measured using an MTT assay. Expression of the three cytokines from osteoblasts,
receptor activator of nuclear factor-κB ligand (RANKL), osteoprotegerin (OPG), and macrophage colony-stimulating factor (M-CSF), were analyzed
by real-time polymerase chain reaction and enzyme-linked immunosorbent assay.
Results: Cell viability was decreased to 82.75%±1.00% by alendronate and then increased to 110.43%±1.35% after treatment with rhBMP-2 (P<0.05, respectively). OPG, RANKL, and M-CSF expression were all decreased by alendronate treatment. RANKL and M-CSF expression were increased,
but OPG was not significantly affected by rhBMP-2.
Conclusion: rhBMP2 does not affect OPG gene expression in hFOB, but it may increase RANKL and M-CSF gene expression.
목차
I. Introduction
II. Materials and Methods
III. Results
IV. Discussion
V. Conclusion
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